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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216117Generated: November 2, 2026

Ethyl isocyanatoacetate → HCID 145857606, compound

https://huagongshe.com/reaction/2216117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanatoacetateHCID 76283—
ReactantHCID 145857630HCID 145857630—
SolventDichloromethaneHCID 6344—
ProductHCID 145857606HCID 14585760686%

Reaction Steps

A solution of [(4-{2′-[3-(2-amino-ethyl)-ureido]-6′-methyl-biphenyl-3-sulfonyl}-5-methylsulfanyl-thiophen-2-yl)-imino-methyl]-carbamic acid tert-butyl ester ((Example 194: step a) 0.030 g, 0.050 mmol) in CH2Cl2 (10 mL) was treated with ethyl isocyanatoacetate (6.70 μL, 0.060 mmol) and stirred at room temperature 35 min. The reaction was diluted with CH2Cl2 and washed with water (1×15 mL). The organic layer was dried over MgSO4 and concentrated in vacuo to afford the product {3-[2-(3-{3′-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-6-methyl-biphenyl-2-yl}-ureido)-ethyl]-ureido}-acetic acid methyl ester (0.031 g, 86%) as an off-white solid. C32H40N6O8S3: 733.21 (M+1) found 732.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109354B2
Source datasetuspto-grants-2006_09
ORD IDord-53e98a921a374875adf2a3bedc54a629
Source noteuspto-grants-2006_09