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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276474Generated: October 30, 2026

2-Methyl-4-nitrophenyl isothiocyanate → HCID 178455883, compound

https://huagongshe.com/reaction/276474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitrophenyl isothiocyanateHCID 145621—
Reactant(2S,3S)-2-Amino-3-methyl-1-pentanolHCID 2724027—
ProductHCID 178455883HCID 178455883—

Reaction Steps

(1S,2S)-1-(Hydroxymethyl)-2-methylbutylamine was converted to (1S,2S)-1-(chloromethyl)-2-methylbutanammonium chloride as described in Method B7a. 2-Methyl-4-nitrophenyl isothiocyanate was reacted with (1S,2S)-1-(chloromethyl)-2-methylbutanammonium chloride according to Method C1a to give (4S)-2-(2-methyl-4-nitrophenylimino)-4-((2S)-2-butyl)-1,3-thiazolidine. The thiazolidine was reacted with isobutyl bromide according to Method D2a to afford (4S)-2-(2-methyl-4-nitrophenylimino)-4-((2S)-2-butyl)-3-isobutyl-1,3-thiazolidine HCl salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-97cc1cc146484f85aa635cd362769fbb
Source noteuspto-grants-2002_03