HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656567Generated: October 30, 2026
Glutamic acid diethyl ester → HCID 178508852, compound
https://huagongshe.com/reaction/1656567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glutamic acid diethyl ester | HCID 73961 | — |
| Reactant | HCID 178471569 | HCID 178471569 | — |
| Product | HCID 178508852 | HCID 178508852 | — |
Reaction Steps
By substituting 4-(4-carbethoxyphenyl)butanal for 3-(4-carbethoxyphenyl)propanal in the procedure of Example 1 and thereafter substituting an equivalent amount of ethyl cyanoacetate for malononitrile in Example 2, there is obtained ethyl 4-[3-(2-amino-3-carbethoxyfur-4-yl)prop-1-yl]benzoate which thereafter is treated with guanidine in free base as described above to yield ethyl 4-[3-(2-amino-4-hydroxypyrrolo[2,3-d]-pyrimidin-5-yl)prop-1-yl]benzoate. This is subjected to saponification to yield 4-[3-(2-amino-4-hydroxypyrrolo[2,3-d]pyrimidin-5-yl)prop-1-yl]benzoic acid which then is coupled with diethyl L-glutamate, and the resulting diethyl N-[4-{3-(2-amino-4-hydroxypyrrolo[2,3-d]-pyrimidin-5-yl)prop-1-yl}benzoyl]-L-glutamate is saponified to yield N-[4-(3-(2-amino-4-hydroxypyrrolo[2,3-d]pyrimidin-5-yl)prop-1-yl}benzoyl]-L-glutamic acid, m.p. 190°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05254687 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-fe43eac206aa45aca16b2fc000b6e8b3 |
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| Source note | uspto-grants-1993_10 |
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