Stearoyl chloride → HCID 20246364, compound

HRID 1589549Notes

Reaction equation

[NH2:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][CH:10]=[C:5]2[C:4](=[O:11])[N:3]=1.[C:12](Cl)(=[O:30])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>>[C:12]([NH:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][CH:10]=[C:5]2[C:4](=[O:11])[N:3]=1)(=[O:30])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]

Participants

Reactant 2

HCID 8212Stearoyl chloride

HCID 219043482-Amino-4H-pyrrolo[2,3-d]pyrimidin-4-one

Product 1

HCID 20246364HCID 20246364, compound

Procedure

Using 2-aminopyrrolo(2,3-d)pyrimidin-4-one and octadecanoyl chloride, the above-identified compound is produced by the same procedure as Reference Example 2.

Workup

customthe above-identified compound is produced by the same procedure as Reference Example 2

Sources & evidence

ORD record: ord-304d384bd25c45298df607478626574d
Source dataset: uspto-grants-1986_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04571423

Reaction notes

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